Determine the necessary mass, volume, or concentration for preparing a solution.
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≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488196281 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488196281 |
| Canonical Smiles | CC(=O)NC1=CC=C(C=C1)C=NNC(=S)N |
| IUPAC Name | N-[4-[(E)-(carbamothioylhydrazinylidene)methyl]phenyl]acetamide |
| InChIKey | SRVJKTDHMYAMHA-WUXMJOGZSA-N |
| INCHI | 1S/C10H12N4OS/c1-7(15)13-9-4-2-8(3-5-9)6-12-14-10(11)16/h2-6H,1H3,(H,13,15)(H3,11,14,16)/b12-6+ |
| Isomeric SMILES | CC(=O)NC1=CC=C(C=C1)/C=N/NC(=S)N |
| PubChem CID | 9568512 |
| Molecular Weight | 236.29 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Anilides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acetanilides |
| Alternative Parents | N-acetylarylamines Thiosemicarbazones Acetamides Secondary carboxylic acid amides Organosulfur compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Acetanilide - N-acetylarylamine - N-arylamide - Thiosemicarbazone - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organic oxide - Organopnictogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as acetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group. |
| External Descriptors | Not available |
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| Melt Point(°C) | 225-230°C |
|---|---|
| Molecular Weight | 236.300 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 236.073 Da |
| Monoisotopic Mass | 236.073 Da |
| Topological Polar Surface Area | 112.000 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 285.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
| 1. Li Yufang, Chen Yunlong, Zi Futing, Hu Xianzhi. (2024) First gold recovery from PCBs through en-thiosulfate leaching and selective adsorption with carbon. BRAZILIAN JOURNAL OF CHEMICAL ENGINEERING, [PMID:] [10.1007/s43153-024-00510-7] |
| 2. Li Jiatong, Song Lei, Zhang Hao, Wang Runnan, Zhu Bo, Lou Dawei. (2025) Thiosemicarbazone-Modified Polysilicate Flocculants for Copper Ion Removal. WATER AIR AND SOIL POLLUTION, 236 (10): (1-16). [PMID:] [10.1007/s11270-025-08232-3] |